Clinical trial Recruiting at 1 site Observational Ages 18 and up

Investigating heart inflammation after a stroke

Official title: Magnetic Resonance Imaging Evidence of Cardiac Inflammation Post-Stroke

Run by London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's · NCT05714618 · Data updated 2026-11-12

This study is trying to see if heart inflammation is linked to strokes by comparing heart health in stroke patients and those with other neurological symptoms.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment44 (estimated)
SponsorLondon Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Academic / other
Locations1 site (London, Ontario)
StatusRecruiting
StartedOctober 1, 2021
Main results expectedJune 16, 2027
Study endsDecember 31, 2027
Registry record updatedSeptember 18, 2026
Trial IDNCT05714618 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are individuals who have experienced an acute ischemic stroke in the middle cerebral artery territory.

Probably not a fit

Patients with a history of significant cardiovascular issues or recent infections may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to enroll 44 patients who have experienced an acute ischemic stroke in the middle cerebral artery, comparing inflammatory markers within 10 days and 60±15 days post-stroke. Additionally, 24 control patients with acute neurological symptoms but no brain infarct will be included for comparison. The study will utilize gadolinium-enhanced cardiac MRI and assess B-Type Natriuretic Peptide and systemic inflammatory markers to understand the relationship between stroke and cardiac inflammation.

Why it matters

Potential benefit: If successful, this study could enhance understanding of cardiac inflammation post-stroke, potentially leading to improved patient management and outcomes.

How similar studies have gone: While this approach is innovative, similar studies have not been widely reported, indicating a novel exploration in this area.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

• Acute ischemic stroke in the right or left MCA territory. Acute ischemic stroke is defined as acute onset focal symptoms matching an acute brain infarct documented on Head computed tomography or diffusion-weighted imaging (DWI) MRI of the brain showing restricted diffusion.

Exclusion Criteria:

* History of known atrial fibrillation, prior myocardial infarction, coronary artery disease, heart failure, prior cardiovascular surgery or percutaneous intervention.
* Previous stroke (occurred within 3 months before the index event)
* Impaired renal function defined as a creatinine clearance \<97 mL/min in men or \<88 mL/min in women, according to the Cockcroft formula.
* hs-TnT \>100 on routine acute stroke baseline bloodwork upon admission.
* Clinically or neurologically unstable patients as per the treating physician.
* Ongoing infection or recent infection within the previous 3 months
* Surgery within 3 months before the stroke
* Concurrent and active inflammatory conditions (connective tissue diseases, rheumatological disease, etc.) or use of anti-inflammatory medications
* Pregnancy, Stage IV renal insufficiency, eGFR \<30, and any other contraindications to the use of gadolinium.
* Stroke with symptomatic hemorrhagic transformation
* Subjects will be excluded if they fail the LHSC standard MRI screening questionnaire (cardiac pacemakers/wires, aneurysm clips, shunt/surgical clips, shrapnel/bullets, dentures or metal braces, intra-uterine devices, heart valves, ear implants, prostheses, medication patches such as Nicoderm, Habitrol, or Transderm-Nitro, claustrophobia, history of a head or eye injury involving metal fragments.

Where it's running

  • Heart & Brain Lab, Western University
    London, Ontario, Canada
    Recruiting

Study contacts

  • Principal investigator: Luciano Sposato, MD — London Health Sciences Center, Western University
  • Study coordinator: Diana Ayan, MSc
  • Email: diana.ayan@lhsc.on.ca
  • Phone: +1 519.685.8500

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.